首页> 外文期刊>The biochemical journal >Acute effects of a β-adrenoceptor agonist (BRL 26830A) on rat brown-adipose-tissue mitochondria. Increased GDP binding and GDP-sensitive proton conductance without changes in the concentration of uncoupling protein
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Acute effects of a β-adrenoceptor agonist (BRL 26830A) on rat brown-adipose-tissue mitochondria. Increased GDP binding and GDP-sensitive proton conductance without changes in the concentration of uncoupling protein

机译:β肾上腺素受体激动剂(BRL 26830A)对大鼠褐色脂肪组织线粒体的急性作用。增加GDP结合力和GDP敏感的质子电导率,而未改变解偶联蛋白的浓度

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pGDP binding, proton conductance and the specific concentration of uncoupling protein were measured in brown-adipose-tissue mitochondria of rats treated acutely with the novel beta-agonist, BRL 26830A. At 1 h after dosing with BRL 26830A, mitochondrial GDP binding was increased more than 2-fold. The increase in binding resulted from an increase in the number of binding sites. An iterative analysis of Scatchard binding data suggested that there is only one high-affinity GDP-binding site (Kd 0.3 microM) in brown-adipose-tissue mitochondria. The acute increase in GDP binding produced by treatment with BRL 26830A occurred without any alteration in the specific mitochondrial concentration of uncoupling protein, as determined by radioimmunoassay. Treatment with the beta-agonist did, however, lead to a small increase in the GDP-sensitive component of mitochondrial proton conductance. These results indicate that GDP-binding sites on uncoupling protein can be rapidly unmasked after treatment with a brown-fat-specific beta-agonist, and that the increase in binding reflects an increase in the activity of the mitochondrial proton-conductance pathway./p
机译:在新型β激动剂BRL 26830A急性处理的大鼠的棕色脂肪组织线粒体中,测量了GDP结合力,质子传导性和解偶联蛋白的特定浓度。在使用BRL 26830A给药1小时后,线粒体GDP结合增加了2倍以上。结合的增加是由于结合位点数目的增加。对Scatchard结合数据的迭代分析表明,棕色脂肪组织线粒体中仅存在一个高亲和力GDP结合位点(Kd 0.3 microM)。通过放射免疫测定法确定,用BRL 26830A处理产生的GDP结合急剧增加,而线联蛋白的解偶联蛋白的特定线粒体浓度没有任何变化。但是,使用β受体激动剂进行的治疗确实导致线粒体质子传导率的GDP敏感成分略有增加。这些结果表明,用棕脂特有的β-激动剂处理后,解偶联蛋白上的GDP结合位点可以迅速被掩盖,结合的增加反映了线粒体质子传导途径的活性增加。 >

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